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Published in 2023 at "Neurology: Genetics"
DOI: 10.1212/nxg.0000000000200037
Abstract: Background and Objectives Missense variants of the valosin-containing protein (VCP) gene cause a progressive, autosomal dominant disease termed VCP multisystem proteinopathy (MSP1). The disease is a constellation of clinical features including inclusion body myopathy (IBM),…
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Keywords:
hispanic families;
r159h vcp;
vcp multisystem;
frontotemporal dementia ... See more keywords